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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 613 (1992), S. 137-148 
    ISSN: 0044-2313
    Keywords: bis(trimethylsilyl)aminosubstituted silanes ; synthesis ; lithium silylamides ; reaction behaviour ; cyclodisilazanes ; crystal structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Reaction Behaviour of Lithiated Aminosilanes RR′Si(H)N(Li)SiMe3The bis(trimethylsilyl)aminosubstituted silances RR′Si(H)N(SiMe3)2 11-16 (R,R′ = Me, Me3SiNH, (Me3Si)2N) are obtained by the reaction of the lithium silylamides RR′Si(H)N(Li)SiMe3 1-10 (R,R′ = Me3SiNLi, Me, Me3SiNH, (M3Si)2N) with chlorotrimethylsilane in the polar solvent tetrahydrofurane (THF). In the reaction of the lithium silylamides [(Me3Si)2N]2(Me3SiNLi)SiH 10 with chlorotrimethylsilane in THF the rearranged product 1,1,3-tris[bis(trimethylsilyl)amino]-3-methyl-1,3-disila-butane [(Me3Si)2N]2Si(H)CH2SiMe2N(SiMe3)2 17 is formed. The reaction of the lithium silyamides RR′ Si(H)N(Li)SiMe3 1-3 (1: R = R′ = Me; 2: R = Me, R′ = Me3SiNH; 3: R = Me, R′ = Me3SiNLi) with chlorotrimethylsilane in the nonpolar solvent n-hexane gives the cyclodisilazanes [RR′ Si—NSiMe3]2 18-22 (R = Me, Me3SiNH, (Me3Si)2N; R′ = Me, Me3SiNH, (Me3Si)2N, N(SiMe3)Si · Me(NHSiMe3)2) and trimethylsilane. The lithium silylamides 4,5,6,9,10 (4: R = R′ = Me3SiNH; 5: R = Me3SiNH, R′ = Me3SiNLi; 6: R = R′ = Me3SiNLi; 9: R = (Me3Si)2N, R ′ = Me3SiNLi; 10: R = R′ = (Me3Si)2N) shows with chlorotrimethylsilane in n-hexane no reaction.The crystal structure of 17 and 21 are reported.
    Notes: Die bis(trimethylsilyl)aminosubstituierten Silane RR′Si(H)N(SiMe3)2 11-16 (R,R′ = Me, Me3SiNH, (Me3Si)2N) entstehen bei der Umsetzung der Lithiumsilylamide RR′Si(H)N(Li)SiMe3 1-10 (R,R′ = Me3SiNLi, Me, Me3SiNH, (M3Si)2N) mit Chlortrimethylsilan im polaren Lösungsmittel Tetrahydrofuran (THF). Das Lithiumsilylamid [(Me3Si)2N]2(Me3SiNLi) · SiH 10 reagiert mit Chlortrimethylsilan in THF unter Umlagerung zum 1,1,3-Tris[bis(trimethylsilyl)amino]-3-methyl-1,3-disila-butan [(Me3Si)2N]2Si(H)CH2SiMe2N · (SiMe3)2 17. Die Reaktion der Lithiumsilylamide RR′Si(H)N(Li)SiMe3 1-3 (1: R = R′ = Me; 2: R = Me, R′ = Me3SiNH; 3: R = Me, R′ = Me3SiNLi) mit Chlortrimethylsilan im unpolaren Lösungsmittel n-Hexan ergibt die Cyclodisilazane [RR′Si—NSiMe3]218-22 (R = Me, Me3SiNH, (Me3Si)2N; R′ = Me, Me3SiNH, (Me3Si)2N, N(SiMe3)SiMe(NHSiMe3)2) und Trimethylsilan. Die Lithiumsilylamide 4,5,6,9,10 (4: R=R′ = Me3SiNH; 5: R = Me3SiNH, R′ = Me3SiNLi; 6: R = R′ = Me3SiNLi; 9: R = (Me3Si)2N, R′ = Me3SiNLi; 10: R = R′ = (Me3Si)2N) zeigen mit Chlortrimethylsilan in n-Hexan keine Reaktion. Die Kristallstrukturen von 17 und 21 werden angegeben.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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